Director, Trial Consent R&D - Office base, Iasi Romania. Teams in Finland and Romania
The role is responsible for development and management of a high-performing TrialConsent (eConsent) R&D that understands the SW development requirements, tools and processes in a regulated environment to reach maximum business velocity.
Directs the company’s TrialConsent software development and technology research activities.
Manages its software and technology development process and ensures continuous improvement of the development process, tools and methodologies.
Directs TrialConsent research and development activities supporting continuity of the company’s technology platform for multiple products/solutions and ensures efficient use of companywide components, tools and practices deployment.
Ensures product development activities alignment with company’s long-term strategy, strategic programs and product roadmaps.
Provides technical assistance and leadership, when necessary.
Works in close co-operation with other units inside and outside the R&D organisation to maximize cross unit synergies, such as business case development support for product management.
About CRF Health
Global Leader in eCOA Solutions
CRF Health is a global leader in eCOA (electronic Clinical Outcome Assessments) solutions for the life sciences industry. eCOA encompasses PROs (Patient Reported Outcomes), ObsROs (Observer Reported Outcomes) and ClinROs (Clinician or Rater Reported Outcomes) with outstanding project management focused on delivering value for our customers. Committed to driving the change to higher quality outcomes and more efficient paper-free clinical trials through improved patient engagement, our intuitive and patient-focused eCOA technology helps companies bring new medicines to market quickly, safely and more cost-effectively. Our complete eCOA solutions are ideal for home and site-based phase I-IV clinical trials across the world for many therapeutic areas and patient populations. More information can be found on our website.